A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8808646



Internal ID13643574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41476385..41480895hg38UCSC Ensembl
Innerchr13:41478375..41479315hg38UCSC Ensembl
Outerchr13:41476275..41481015hg38UCSC Ensembl
chr13:42050521..42055031hg19UCSC Ensembl
Innerchr13:42052511..42053451hg19UCSC Ensembl
Outerchr13:42050411..42055151hg19UCSC Ensembl
chr13:40948521..40953031hg18UCSC Ensembl
Innerchr13:40950511..40951451hg18UCSC Ensembl
Outerchr13:40948411..40953151hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg384511
hg194511
hg184511
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3416043
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8808646
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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